ClinicalDocument/informationRecipient MAY be present. When present, it SHALL be in accordance with the HL7 CDA R2 standard and further constrained by this specification to require the presence of name (on the informationRecipient and/or receivedOrganization), addr and telecom. Additionally, it SHALL have the following: <templateId root="188.8.131.52.4.1.193184.108.40.206.1.4"/> - The templateId element identifies this participant as an intended recipient. The templateId SHALL have root="220.127.116.11.4.1.19318.104.22.168.1.4". The informationRecipient/intendedRecipient element can be multiple. It introduces an intended recipient of the laboratory report, other than the Ordering Provider (described as a referrer participant). These elements carry the list of the originally intended recipients of the laboratory report, i.e. those who were known at the time the report was created and published for sharing.